4.5 Review

Neuronal Migration and AUTS2 Syndrome

期刊

BRAIN SCIENCES
卷 7, 期 5, 页码 -

出版社

MDPI
DOI: 10.3390/brainsci7050054

关键词

Autism; intellectual disabilities; AUTS2 syndrome; Rac1; neuritogenesis; neuronal migration; cytoskeleton; PRC1

资金

  1. Challenging Exploratory Research [15K14337]
  2. Innovative Areas from MEXT [15H01304, 16H06528]
  3. AMED [16dm0107085h0001]
  4. Naito Foundation
  5. Takeda Foundation
  6. Uehara Foundation
  7. Princess Takamatsu Cancer Research fund
  8. Intramural Research Grants for Neurological and Psychiatric Disorders of NCNP [27-7, 28-4]
  9. [15H04268]
  10. [16K07021]
  11. Grants-in-Aid for Scientific Research [15H01304, 16K21734, 15K14337, 16H06528, 16K07021, 16H06524] Funding Source: KAKEN

向作者/读者索取更多资源

Neuronal migration is one of the pivotal steps to form a functional brain, and disorganization of this process is believed to underlie the pathology of psychiatric disorders including schizophrenia, autism spectrum disorders (ASD) and epilepsy. However, it is not clear how abnormal neuronal migration causes mental dysfunction. Recently, a key gene for various psychiatric diseases, the Autism susceptibility candidate 2 (AUTS2), has been shown to regulate neuronal migration, which gives new insight into understanding this question. Interestingly, the AUTS2 protein has dual functions: Cytoplasmic AUTS2 regulates actin cytoskeleton to control neuronal migration and neurite extension, while nuclear AUTS2 controls transcription of various genes as a component of the polycomb complex 1 (PRC1). In this review, we discuss AUTS2 from the viewpoint of human genetics, molecular function, brain development, and behavior in animal models, focusing on its role in neuronal migration.

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